Align Homocysteine/cysteine synthase; O-acetylserine/O-acetylhomoserine sulfhydrylase; OAS-OAH SHLase; OAS-OAH sulfhydrylase; EC 2.5.1.47; EC 2.5.1.49 (characterized)
to candidate WP_013644806.1 METBO_RS06070 O-acetylhomoserine aminocarboxypropyltransferase/cysteine synthase family protein
Query= SwissProt::P06106 (444 letters) >NCBI__GCF_000191585.1:WP_013644806.1 Length = 439 Score = 439 bits (1128), Expect = e-127 Identities = 221/438 (50%), Positives = 300/438 (68%), Gaps = 21/438 (4%) Query: 7 TVQLHAGQENPGDNAHRSRAVPIYATTSYVFENSKHGSQLFGLEVPGYVYSRFQNPTSNV 66 T+ LH GQE P D+A SRAVPIY T+SYVF +++H + LFGL G +Y+R NPT++V Sbjct: 17 TIGLHVGQEEP-DSATGSRAVPIYLTSSYVFNDTEHAANLFGLREFGNIYTRIMNPTTDV 75 Query: 67 LEERIAALEGGAAALAVSSGQAAQTLAIQGLAHTGDNIVSTSYLYGGTYNQFKISFKRFG 126 E+R+AA+EGGA AL V+SG +A LA+ ++ G+NIVS LYGGTY F + R G Sbjct: 76 FEKRVAAVEGGATALGVASGMSAIFLAVLNVSELGENIVSGDNLYGGTYELFNYTLPRLG 135 Query: 127 IEARFVEGDNPEEFEKVFDERTKAVYLETIGNPKYNVPDFEKIVAIAHKHGIPVVVDNTF 186 +FV + PEEFE DE+T+A+Y+E++GNPK +VPDFEK+ IAH H IP++VDNT Sbjct: 136 RTVKFVNSEKPEEFEAAIDEKTRAIYVESLGNPKLDVPDFEKLAKIAHDHDIPLIVDNTS 195 Query: 187 GAGGYFCQPIKYGADIVTHSATKWIGGHGTTIGGIIVDSGKFPWKDYPEKFPQFSQPAEG 246 G +PI YGADI SATK+IGGHGT+IGG+IVDSGKF W + KFPQF+ P Sbjct: 196 TVG--LLRPIDYGADITVISATKYIGGHGTSIGGVIVDSGKFNWGN--GKFPQFTDPDPS 251 Query: 247 YHGTIYNEAY------GNLAYIVHVRTELLRDLGPLMNPFASFLLLQGVETLSLRAERHG 300 YHG Y E + GN+A+ + R LLRDLGP ++PF +F LQG+ETL LR +H Sbjct: 252 YHGLKYWETFGDFPGAGNIAFTIRARVVLLRDLGPALSPFNAFQFLQGLETLELRVLKHA 311 Query: 301 ENALKLAKWLEQSPYVSWVSYPGLASHSHHENAKKYLSNGFGGVLSFGVKDLPNADKETD 360 ENALK+AK L+ P VSW++YPGL HE A KYL G+GG++ FG++ Sbjct: 312 ENALKVAKHLKNHPKVSWINYPGLEEDPRHEVASKYLKGGYGGLIGFGIEGGLE------ 365 Query: 361 PFKLSGAQVVDNLKLASNLANVGDAKTLVIAPYFTTHKQLNDKEKLASGVTKDLIRVSVG 420 SG + ++N++L S+LAN+GD+K+LVI P TTH+QL +E+ +GVT+D +R+S+G Sbjct: 366 ----SGKKFIENVELFSHLANIGDSKSLVIHPASTTHQQLTREEQETTGVTEDFVRLSIG 421 Query: 421 IEFIDDIIADFQQSFETV 438 +E ++DIIAD Q+ + Sbjct: 422 LEDVEDIIADIDQALSKI 439 Lambda K H 0.317 0.136 0.402 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 593 Number of extensions: 22 Number of successful extensions: 6 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 444 Length of database: 439 Length adjustment: 32 Effective length of query: 412 Effective length of database: 407 Effective search space: 167684 Effective search space used: 167684 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.6 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory